Taiwan FDA registration 376d62af101bb16747c68d2f6c9b25ca

Longsheng pregnancy test reagent

TW: 龍生驗孕試劑

Taiwan·Risk Class 2·ACON BIOTECH (HANGZHOU) CO., LTD.·Registered May 02, 2006 – May 02, 2011Cancelled

Registration details

Analysis ID: 376d62af101bb16747c68d2f6c9b25ca
Customs Code: DHA04200022603

Company information

Manufacturer: ACON BIOTECH (HANGZHOU) CO., LTD.
Manufacturer Country: China
Authorized Representative: DRAGON PHARMACEUTICAL CO., LTD.

Product details

Intended Use: Urine and serum are tested for the intensity of human pilionic gonadotropin.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1155 Human chorionic gonadotropin testing system
Import Information: Chinese goods;; input

Dates and status

Registration Date: May 02, 2006
Expiry Date: May 02, 2011
Cancellation Date: Nov 09, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Longsheng pregnancy test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 376d62af101bb16747c68d2f6c9b25ca and manufactured by ACON BIOTECH (HANGZHOU) CO., LTD.. The authorized representative in Taiwan is DRAGON PHARMACEUTICAL CO., LTD..

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